These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

251 related articles for article (PubMed ID: 9063735)

  • 1. Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndrome.
    Lo Nigro C; Chong CS; Smith AC; Dobyns WB; Carrozzo R; Ledbetter DH
    Hum Mol Genet; 1997 Feb; 6(2):157-64. PubMed ID: 9063735
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A revision of the lissencephaly and Miller-Dieker syndrome critical regions in chromosome 17p13.3.
    Chong SS; Pack SD; Roschke AV; Tanigami A; Carrozzo R; Smith AC; Dobyns WB; Ledbetter DH
    Hum Mol Genet; 1997 Feb; 6(2):147-55. PubMed ID: 9063734
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Alteration of the LIS1 gene in Japanese patients with isolated lissencephaly sequence or Miller-Dieker syndrome.
    Sakamoto M; Ono J; Okada S; Masuno M; Nakamura Y; Kurahashi H
    Hum Genet; 1998 Nov; 103(5):586-9. PubMed ID: 9860301
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Refinement of a 400-kb critical region allows genotypic differentiation between isolated lissencephaly, Miller-Dieker syndrome, and other phenotypes secondary to deletions of 17p13.3.
    Cardoso C; Leventer RJ; Ward HL; Toyo-Oka K; Chung J; Gross A; Martin CL; Allanson J; Pilz DT; Olney AH; Mutchinick OM; Hirotsune S; Wynshaw-Boris A; Dobyns WB; Ledbetter DH
    Am J Hum Genet; 2003 Apr; 72(4):918-30. PubMed ID: 12621583
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The location and type of mutation predict malformation severity in isolated lissencephaly caused by abnormalities within the LIS1 gene.
    Cardoso C; Leventer RJ; Matsumoto N; Kuc JA; Ramocki MB; Mewborn SK; Dudlicek LL; May LF; Mills PL; Das S; Pilz DT; Dobyns WB; Ledbetter DH
    Hum Mol Genet; 2000 Dec; 9(20):3019-28. PubMed ID: 11115846
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Murine modelling of classical lissencephaly.
    Gambello MJ; Hirotsune S; Wynshaw-Boris A
    Neurogenetics; 1999 Apr; 2(2):77-86. PubMed ID: 10369882
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Deletion of 17p13 and LIS1 gene mutation in isolated lissencephaly sequence.
    Elias RC; Galera MF; Schnabel B; Briones MR; Borri ML; Lipay M; Carvalheira G; Brunoni D; Melaragno MI
    Pediatr Neurol; 2006 Jul; 35(1):42-6. PubMed ID: 16814084
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genomic organization of the murine Miller-Dieker/lissencephaly region: conservation of linkage with the human region.
    Hirotsune S; Pack SD; Chong SS; Robbins CM; Pavan WJ; Ledbetter DH; Wynshaw-Boris A
    Genome Res; 1997 Jun; 7(6):625-34. PubMed ID: 9199935
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 14-3-3 epsilon has no homology to LIS1 and lies telomeric to it on chromosome 17p13.3 outside the Miller-Dieker syndrome chromosome region.
    Chong SS; Tanigami A; Roschke AV; Ledbetter DH
    Genome Res; 1996 Aug; 6(8):735-41. PubMed ID: 8858348
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Intragenic deletions and duplications of the LIS1 and DCX genes: a major disease-causing mechanism in lissencephaly and subcortical band heterotopia.
    Haverfield EV; Whited AJ; Petras KS; Dobyns WB; Das S
    Eur J Hum Genet; 2009 Jul; 17(7):911-8. PubMed ID: 19050731
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Fluorescence in situ hybridization analysis with LIS1 specific probes reveals a high deletion mutation rate in isolated lissencephaly sequence.
    Pilz DT; Macha ME; Precht KS; Smith AC; Dobyns WB; Ledbetter DH
    Genet Med; 1998; 1(1):29-33. PubMed ID: 11261426
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Microdeletions of chromosome 17p13 as a cause of isolated lissencephaly.
    Ledbetter SA; Kuwano A; Dobyns WB; Ledbetter DH
    Am J Hum Genet; 1992 Jan; 50(1):182-9. PubMed ID: 1346078
    [TBL] [Abstract][Full Text] [Related]  

  • 13. LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation.
    Pilz DT; Matsumoto N; Minnerath S; Mills P; Gleeson JG; Allen KM; Walsh CA; Barkovich AJ; Dobyns WB; Ledbetter DH; Ross ME
    Hum Mol Genet; 1998 Dec; 7(13):2029-37. PubMed ID: 9817918
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Lissencephaly. A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13.
    Dobyns WB; Reiner O; Carrozzo R; Ledbetter DH
    JAMA; 1993 Dec; 270(23):2838-42. PubMed ID: 7907669
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Differences in the gyral pattern distinguish chromosome 17-linked and X-linked lissencephaly.
    Dobyns WB; Truwit CL; Ross ME; Matsumoto N; Pilz DT; Ledbetter DH; Gleeson JG; Walsh CA; Barkovich AJ
    Neurology; 1999 Jul; 53(2):270-7. PubMed ID: 10430413
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Analysis of lissencephaly-causing LIS1 mutations.
    Sapir T; Eisenstein M; Burgess HA; Horesh D; Cahana A; Aoki J; Hattori M; Arai H; Inoue K; Reiner O
    Eur J Biochem; 1999 Dec; 266(3):1011-20. PubMed ID: 10583396
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel inverted 17p13.3 microduplication disrupting PAFAH1B1 (LIS1) in a girl with syndromic lissencephaly.
    Classen S; Goecke T; Drechsler M; Betz B; Nickel N; Beier M; Schaper J; Karenfort M; Royer-Pokora B
    Am J Med Genet A; 2013 Jun; 161A(6):1453-8. PubMed ID: 23633430
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 14-3-3epsilon is important for neuronal migration by binding to NUDEL: a molecular explanation for Miller-Dieker syndrome.
    Toyo-oka K; Shionoya A; Gambello MJ; Cardoso C; Leventer R; Ward HL; Ayala R; Tsai LH; Dobyns W; Ledbetter D; Hirotsune S; Wynshaw-Boris A
    Nat Genet; 2003 Jul; 34(3):274-85. PubMed ID: 12796778
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The lissencephaly gene product Lis1, a protein involved in neuronal migration, interacts with a nuclear movement protein, NudC.
    Morris SM; Albrecht U; Reiner O; Eichele G; Yu-Lee LY
    Curr Biol; 1998 May; 8(10):603-6. PubMed ID: 9601647
    [TBL] [Abstract][Full Text] [Related]  

  • 20. NudE-L, a novel Lis1-interacting protein, belongs to a family of vertebrate coiled-coil proteins.
    Sweeney KJ; Prokscha A; Eichele G
    Mech Dev; 2001 Mar; 101(1-2):21-33. PubMed ID: 11231056
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.